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FENOFIBRATE

NDC 51655-009, FENOFIBRATE, tablet, from Northwind Health Company, LLC.

Product NDC
51655-009
Status
Listed
Labeler
Northwind Health Company, LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA076509
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51655-009 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FENOFIBRATE160 mg/1

Pharmacologic classes

Peroxisome Proliferator Receptor alpha Agonist [EPC]

Package NDCNDC-11Package
51655-009-525165500095230 TABLET in 1 BOTTLE, DISPENSING (51655-009-52)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/4b4447a1-8136-4258-b2c8-c5f9c1bcec92

Use it

Look up 51655-009 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51655-009 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51655-009. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.